View Clinical Trial (Medical Research Study)
Effect of Pantoprazole 40mg Daily vs Placebo on Power Spectral Analysis of the Sleep Electroencephalogram (EEG) of Patients With Gastroesophageal Reflux Disease (GERD) - NCT00674245-85723(Clinical Trial 219403)
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| City: |
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Tucson |
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State:
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AZ |
| Zip Code: |
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85723 |
| Conditions: |
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Gastroesophageal Reflux Disease |
| Purpose: |
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The purpose of this research study is to determine if treatment with pantoprazole 40 mg
daily versus a placebo improves sleep quality in patients with gastroesophageal reflux
disease (GERD). Another purpose is to determine if treatment with pantoprazole 40 mg once
daily versus a placebo improves sleep outcomes in patients with gastroesophageal reflux
disease using spectral analysis of sleep electroencephalogram (EEG).
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| Study summary: |
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It appears that the presence of intraesophageal stimuli alone may not be sufficient to
elicit symptoms of heartburn. Most acid reflux events (>80%-90%) do not reach conscious
level and thus are not perceived.[3] It is yet to be determined what factors enhance our
perception of esophageal stimuli and may help to elevate them to the conscious level. In
recent years, central and peripheral factors that may enhance our perception of
intraesophageal stimuli have been evaluated. Intraduodenal fat infusion was shown to enhance
perception of intraesophageal acid in patients with GERD.[4] This study suggested that fat
is an important modulator of postprandial GERD symptoms. Central factors, such as stress and
psychological comorbidity, also appear to have an important role in symptom generation in
patients with GERD, regardless if esophageal inflammation is present or absent.[5-8] Thus,
by modulating brain-gut interactions, perception of pathological and probably physiological
events in the esophagus of patients with GERD may be altered.
Poor sleep is a central factor that may enhance perception of intraesophageal stimuli and
thus elevate them to the conscious level. Several studies have demonstrated that patients
with fibromyalgia or irritable bowel syndrome report increased symptoms due to sleep
abnormalities.[9, 10] Similar reports in patients with GERD are not available. A subset of
patients with GERD experience nocturnal heartburn that may awaken them during the night. In
others, despite lack of nocturnal symptoms, sleep abnormalities may occur due to acid reflux
events. In both cases, GERD leads to poor sleep, and that in turn may enhance perception of
intraesophageal stimuli, leading to reports of increased frequency and severity of perceived
GERD symptoms. Thus, poor sleep may be a crucial factor in symptom generation and
exacerbation of patients with GERD.
Recently, we have used a novel technique, power spectral analysis of the sleep
electroencephalogram (EEG), to assess patients with heartburn and erosive esophagitis and
those with heartburn but without erosive esophagitis.[11] We were able to show that among
heartburn patients with GERD, EEG spectral power during sleep is shifted towards higher
frequencies as compared to heartburn patients without GERD despite similar sleep
architecture.
Several recent therapeutic trials in GERD patients have failed to demonstrate improvement in
polysomnographic studies despite improvement in GERD-related symptoms and subjective reports
of sleep quality.[12] Spectral analysis of the sleep EEG might be a more sensitive tool than
polysomnographic study in assessing objective improvement of sleep in patients receiving
antireflux treatment.
In summary, sleep disturbances in patients with GERD are poorly recognized and rarely
elicited during clinic visits despite their significant impact on patients' quality of life
and probably perception of disease severity. Several studies have demonstrated improvement
of subjective reports of sleep quality in patients with GERD receiving antireflux treatment.
However, the effect of potent antireflux therapy on objective sleep parameters has yet to be
demonstrated. |
| Criteria: |
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Inclusion Criteria:
- 18 to 80 yrs of age
- 2 to 3 episodes of GERD/week
- erosive esophagitis or abnormal 24 hr pH
- able to read and understand, complete questionnaires
Exclusion Criteria:
- barrett's esophagus or peptic stricture on endoscopy
- normal EGD and normal 24 hour pH
- previous upper GI surgery
- comorbidity (cardiovascular, respiratory, renal, hepatic)
- use of narcotics or pain medication on regular basis
- insomnia, shift work sleep disorder, sleep apnea, restless leg syndrome
- diabetes, scleroderma or neuromuscular disorders |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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August 16, 2010 |
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